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Apatite nanoparticles strongly improve red blood cell cryopreservation by mediating trehalose delivery via enhanced membrane permeation

  • Datos identificativos

    Identificador: PC:2924
  • Autores:

    Baulin, V.
    Stefanic, M.
    Ward, K.
    Tawfik, H.
    Seemann, R.
    Guo, Y.
    Fleury, J.-B.
    Drouet, C.
  • Otros:

    Autor según el artículo: Baulin, V.; Stefanic, M.; Ward, K.; Tawfik, H.; Seemann, R.; Guo, Y.; Fleury, J.-B.; Drouet, C.
    Departamento: Enginyeria Química
    Autor/es de la URV: BAULIN, VLADIMIR; Stefanic, M.; Ward, K.; Tawfik, H.; Seemann, R.; GUO, YACHONG; Fleury, J.-B.; Drouet, C.
    Palabras clave: Lipid bilayer Cryopreservation Apatite
    Resumen: Cryopreservation of red blood cells (RBC) is an important method for maintaining an inventory of rare RBC units and managing special transfusion circumstances. Currently, in a clinical setting, glycerol is used as cryoprotectant against freezing damage. After thawing and before transfusion, glycerol must however be removed to avoid intravascular hemolysis, via a complex and time-consuming deglycerolization process which requires specialized equipment. Improved cryopreservation methods using non-toxic agents are required to increase biocompatibility and decrease processing time. Biocompatible cryoprotectants (e.g. trehalose) were proposed, but their low permeation through RBC membranes limits their cryoprotection efficacy. Herein, we report for the first time a glycerol-free cryopreservation approach, using colloidal bioinspired apatite nanoparticles (NP) as bioactive promoters of RBC cryopreservation mediated by trehalose. Addition of apatite NP in the medium tremendously increases RBC cryosurvival, up to 91% (42% improvement compared to a control without NP) which is comparable to FDA-approved cryoprotection protocol employing glycerol. NP concentration and incubation conditions strongly modulate the NP bioactivity. Complementary experimental and computational analyses of the interaction between apatite NP and model lipid bilayers revealed complex events occurring at the NP-bilayer interface. Apatite NP do not cross the bilayer but momentarily modulate its physical status. These changes affect the membrane behavior, and promote the permeation of trehalose and a model fluorescent molecule (FITC). This approach is a new alternative to using toxic glycerol for cells cryopreservation, and the identification of this enhancing no-pore permeation mechanism of apatite NP appears as an original delivery pathway for cryoprotectant agents and beyond.
    Grupo de investigación: Molecular simulation I: Complex Systems
    Áreas temáticas: Chemical engineering Ingeniería química Enginyeria química
    Acceso a la licencia de uso: https://creativecommons.org/licenses/by/3.0/es/
    ISSN: 0142-9612
    Identificador del autor: 0000-0003-2086-4271; ; ; ; ; ; ;
    Fecha de alta del registro: 2017-10-23
    Página final: 149
    Volumen de revista: 140
    Versión del articulo depositado: info:eu-repo/semantics/acceptedVersion
    Enlace a la fuente original: https://www.sciencedirect.com/science/article/pii/S0142961217304179
    Programa de financiación: european; Marie Curie; DFG; SFB1027 european; Marie Curie; ITN; SNAL 608184
    DOI del artículo: 10.1016/j.biomaterials.2017.06.018
    Entidad: Universitat Rovira i Virgili
    Año de publicación de la revista: 2017
    Página inicial: 138
    Tipo de publicación: Article Artículo Article
  • Palabras clave:

    Cèl·lules sanguínies-Crioconservació
    Apatita
    Lipid bilayer
    Cryopreservation
    Apatite
    Chemical engineering
    Ingeniería química
    Enginyeria química
    0142-9612
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